Investigation of synapses in the cortical white matter in human temporal lobe epilepsy

Brain Res. 2022 Mar 15:1779:147787. doi: 10.1016/j.brainres.2022.147787. Epub 2022 Jan 15.

Abstract

Temporal lobe epilepsy (TLE) is one of the most common focal pharmacotherapy-resistant epilepsy in adults. Previous studies have shown significantly higher numbers of neurons in the neocortical white matter in TLE patients than in controls. The aim of this work was to investigate whether white matter neurons are part of the neuronal circuitry. Therefore, we studied the distribution and density of synapses in surgically resected neocortical tissue of pharmacotherapy-resistant TLE patients. Neocortical white matter of temporal lobe from non-epileptic patients were used as controls. Synapses and neurons were visualized with immunohistochemistry using antibodies against synaptophysin and NeuN, respectively. The presence of synaptophysin in presynaptic terminals was verified by electron microscopy. Quantification of immunostaining was performed and the data of the patients' cognitive tests as well as clinical records were compared to the density of neurons and synapses. Synaptophysin density in the white matter of TLE patients was significantly higher than in controls. In TLE, a significant correlation was found between synaptophysin immunodensity and density of white matter neurons. Neuronal as well as synaptophysin density significantly correlated with scores of verbal memory of TLE patients. Neurosurgical outcome of TLE patients did not significantly correlate with histological data, although, higher neuronal and synaptophysin densities were observed in patients with favorable post-surgical outcome. Our results suggest that white matter neurons in TLE patients receive substantial synaptic input and indicate that white matter neurons may be integrated in epileptic neuronal networks responsible for the development or maintenance of seizures.

Keywords: Epileptic seizures; Neuronal network; Subplate; Synaptophysin; White matter neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Resistant Epilepsy / physiopathology*
  • Drug Resistant Epilepsy / surgery
  • Epilepsy, Temporal Lobe / physiopathology*
  • Epilepsy, Temporal Lobe / surgery
  • Humans
  • Neocortex / physiopathology*
  • Neocortex / surgery
  • Nerve Net / physiopathology*
  • Neurons / physiology*
  • Synapses / physiology*
  • Synaptophysin / metabolism
  • Verbal Learning / physiology
  • White Matter

Substances

  • SYP protein, human
  • Synaptophysin